The complement alternative pathway in paroxysmal nocturnal hemoglobinuria: From a pathogenic mechanism to a therapeutic target
Author:
Affiliation:
1. AORN San Giuseppe Moscati Avellino Italy
2. Federico II University of Naples Naples Italy
3. Severe Aplastic Anemia Working Party of the European Society for Blood and Marrow Transplantation Leiden Netherlands
Publisher
Wiley
Subject
Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/imr.13137
Reference109 articles.
1. Paroxysmal nocturnal hemoglobinuria: natural history of disease subcategories
2. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
3. Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene.
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